Ghent University Academic Bibliography

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The transcription factor FOXL2 in ovarian function and dysfunction

Elfride De Baere (UGent) , Marc Fellous and Reiner A Veitia

(2009) FOLIA HISTOCHEMICA ET CYTOBIOLOGICA. 47(5). p.S43-S49
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Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome

DIANE BEYSEN (UGent) , Sarah De Jaegere (UGent) , David Amor, Philippe Bouchard, Sophie Christin-Maitre, Marc Fellous, Philippe Touraine, Arthur W Grix, Raoul Hennekam, Françoise Meire (UGent) , et al.

(2008) HUMAN MUTATION. 29(11). p.E205-E219
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Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction

Elfride De Baere (UGent) , Silvia Copelli, Sandrine Caburet, Paul Laissue, DIANE BEYSEN (UGent) , Sophie Christin-Maitre, Philippe Bouchard, Reiner Veita and Marc Fellous

(2005) PEDIATRIC ENDOCRINOLOGY REVIEWS. 2(4). p.653-660
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- Journal Article
- A1
- open access
Foxl2 gene and the development of the ovary : a story about goat, mouse, fish and woman

Daniel Baron, Frank Batista, Stéphane Chaffaux, Julie Cocquet, Corinne Cotinot, Edmond Cribiu, Elfride De Baere (UGent) , Yann Guiguen, Francis Jaubert, Eric Pailhoux, et al.

(2005) REPRODUCTION NUTRITION DEVELOPMENT. 45(3). p.377-382
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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome

DIANE BEYSEN (UGent) , Jeroen Raes (UGent) , Bart Leroy (UGent) , A Lucassen, JRW Yates, J Clayton-Smith, H Ilyina, SS Brooks, S Christin-Maitre, Marc Fellous, et al.

(2005) AMERICAN JOURNAL OF HUMAN GENETICS. 77(2). p.205-218
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FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

Elfride De Baere (UGent) , DIANE BEYSEN (UGent) , Christine Oley, Birgit Lorenz, Julie Cocquet, Petra De Sutter (UGent) , Koen Devriendt, Michael Dixon, Marc Fellous, Jean-Pierre Fryns, et al.

(2003) AMERICAN JOURNAL OF HUMAN GENETICS. 72(2). p.478-487
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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation

Elfride De Baere (UGent) , Michael J Dixon, Kent W Small, Ethylin W Jabs, Bart Leroy (UGent) , Koenraad Devriendt, Yves Gillerot, Geert Mortier (UGent) , Françoise Meire (UGent) , Lioinel Van Maldergem, et al.

(2001) HUMAN MOLECULAR GENETICS. 10(15). p.1591-1600

Academic Bibliography

The transcription factor FOXL2 in ovarian function and dysfunction

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome

Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction

Foxl2 gene and the development of the ovary : a story about goat, mouse, fish and woman

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation

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